A new study in Nature Communications proposes a method to extend polygenic scores, the estimate of genetic risk factors and a cornerstone of the personalized medicine revolution, to individuals with multiple ancestral origins. The study was led by Dr. Davide Marnetto from the Institute of Genomics of the University of Tartu, Estonia and coordinated by Dr. Luca Pagani from the same institution and from the University of Padova, Italy.
"The information contained in our DNA is a mosaic of genetic instructions inherited from our ancestors, and in many societies one's ancestors often come from the opposite corners of the world." says Dr. Davide Marnetto, first author of the study.
The genome from an admixed individual (blue/red) is separated into the two main ancestral components (Ancestry Deconvolution). Mutations associated with diseases or phenotypic traits on each component (black dots) are studied separately and two Ancestry Specific Partial Polygenic Scores (A and B) are computed using information from population specific Genome Wide Association Studies (GWAS). The two Ancestry Specific Partial Polygenic Scores are then combined together to obtain the individual's Ancestry Specific Polygenic Score.
Credit: Davide Marnetto
The contribution of one's ancestry, or ancestries, to the total risk of developing a specific disease or presenting a given trait is a long standing question of medical genomics. Nevertheless, most of the genotype/phenotype association data come from relatively uniform populations, in order to have a simplified and clearer picture.
But what can be done when dealing with individuals who derive their ancestry from two or more distantly related populations?
"The latest developments of personalized medicine needed an extra step to be applied to individuals with more diverse origins, and here we tried to combine knowledge from homogeneous populations into a model that could work for recently admixed individuals" continues Dr. Marnetto.
To separate the various genomic components of each individual, Marnetto and colleagues applied methods from molecular anthropology and population genomics.
"This research is a welcomed example of deep synergy between evolutionary/population genetics framework and medically oriented large scale genomics science, which is one of the focuses of our institute." says Dr. Mait Metspalu who is heading the institute of Genomics at the University of Tartu.
"Our work provides a solid proof of principle on the feasibility of using population genetic and molecular anthropology to boost the potential of personalized medicine. I hope our work can bring individuals of mixed ancestry one step closer to the benefits of personalized and predictive healthcare" concludes Dr. Luca Pagani, the research coordinator.
Davide Marnetto | EurekAlert!
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